Sall4 isoforms act during proximal-distal and anterior-posterior axis formation in the mouse embryo.
Genesis
2008
46
463-477
The novel mouse mutation Oblivion inactivates the PMCA2 pump and causes progressive hearing loss.
PLoS Genet.
2008
4
Deletion of glucose transporter GLUT8 in mice increases locomotor activity.
Behav. Genet.
2008
38
396-406
Mutation in a novel connexin-like gene (Gjf1) in the mouse affects early lens development and causes a variable small-eye phenotype.
Invest. Ophthalmol. Vis. Sci.
2008
49
1525-1532
Variation of the response to the optokinetic drum among various strains of mice.
Front. Biosci.
2008
13
6269-6275
A phenotype-driven ENU mutagenesis screen for the identification of dominant mutations involved in alcohol consumption.
Mamm. Genome
2008
19
77-84
Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects.
Nat. Genet.
2008
40
963-970
MausDB: An open source application for phenotype data and mouse colony management in large-scale mouse phenotyping projects.
BMC Bioinformatics
2008
9
ER stress-mediated apoptosis in a new mouse model of Osteogenesis imperfecta.
PLoS Genet.
2008
4
A Myo6 mutation destroys coordination between the myosin heads, revealing new functions of myosin VI in the stereocilia of mammalian inner ear hair cells.
PLoS Genet.
2008
4